Latest Research Associate Jobs

Senior Medical Director, Oncology Clinical Development - Lung

Senior physician leader providing medical oversight, safety monitoring and clinical insight across lung cancer studies, from protocol design through data interpretation. Serves on the Clinical Matrix Team, contributes to regulatory interactions and external scientific engagement, and mentors Medical Directors within the programme. Requires deep lung cancer drug development expertise, including early phase trials.

GSK USA - Pennsylvania - Upper Providence US$242,550 – US$404,250 pa

On-site

Medical Director, Oncology Clinical Development - Lung & Head/Neck Cancers

Serves as the physician within oncology clinical programme teams for lung and head/neck cancers, leading medical monitoring, safety oversight and clinical data interpretation across Phase I–III studies. Partners with a Senior Scientist and cross-functional matrix teams on protocol development, regulatory interactions and investigator engagement, with on-site presence 2–3 days per week.

GSK USA - Pennsylvania - Upper Providence US$222,750 – US$371,250 pa

On-site

Medical Director, Oncology Clinical Development - GU

Serves as the physician within a clinical program team, leading medical monitoring and safety oversight for genitourinary oncology studies. Interprets clinical and safety data, contributes to protocol development and regulatory interactions, and acts as a core member of the Clinical Matrix Team. May guide other physicians on complex multi-study programs.

GSK USA - Pennsylvania - Upper Providence US$189,750 – US$316,250 pa

Hybrid

Medical Director-Oncology Clinical Development - GI

Serves as the physician within an oncology clinical programme team, leading medical monitoring and safety oversight for GI cancer studies. Interprets clinical and safety data, contributes to protocol development, and engages investigators, KEEs and health authorities. A core member of the Clinical Matrix Team, providing medical guidance within a matrixed pharma R&D environment.

GSK USA - Pennsylvania - Upper Providence US$222,750 – US$371,250 pa

On-site

Medical Director, Oncology Clinical Development - Hematology

Serves as the physician on a clinical program team, leading medical monitoring, safety oversight and data interpretation for oncology and hematology studies. Partners with a Senior Scientist and cross-functional groups on protocol development, regulatory interactions and investigator engagement within a matrix team. May guide other physicians on complex multi-study programs.

GSK Waltham, United States US$222,750 – US$371,250 pa

Hybrid

Medical Director, Oncology Clinical Development - Hematology

Serves as the physician on a clinical program team, leading medical monitoring and safety oversight for oncology and hematology studies. Interprets clinical and safety data, contributes to protocol development and regulatory interactions, and acts as a core member of the Clinical Matrix Team. May mentor other physicians on complex multi-study programs.

GSK Stevenage

Hybrid

Medical Director, Oncology Clinical Development - Hematology

Serves as the physician on a clinical program team, leading medical monitoring and safety oversight for oncology and hematology studies. Interprets clinical and safety data, contributes to protocol development, and engages investigators, regulators and cross-functional matrix teams. May guide other physicians on complex multi-study programs.

GSK London

Hybrid

Medical Director, Oncology Clinical Development - Hematology

Serves as the physician on a clinical program team, leading medical monitoring and safety oversight for oncology and hematology studies. Interprets clinical and safety data, contributes to protocol development, and engages with investigators, regulators, and cross-functional matrix teams. May guide other physicians on complex multi-study programs.

GSK Mississauga, Canada US$222,750 – US$371,250 pa

Hybrid

Manager, Medical Writing, Immunology

Leads the preparation and finalisation of clinical documents within the Regulatory Medical Writing team, supporting the Immunology therapeutic area. Takes a lead role on assigned projects for content, scientific strategy, timing and tracking, and manages direct reports including hiring, goal-setting and development. Involves guiding cross-functional teams, peer review and maintaining knowledge of ICH and regulatory guidelines.

Johnson & Johnson Innovative Medicine Maidenhead

Medical Director, Oncology Clinical Development - Hematology

Serves as the physician within oncology clinical program teams, leading medical monitoring, safety oversight, and clinical data interpretation across studies. Partners with Senior Scientists and cross-functional matrix teams on protocol development, regulatory interactions, and investigator engagement. May guide other physicians on complex multi-study programs within the clinical strategy set by the Clinical Development Lead.

GSK USA - Pennsylvania - Upper Providence US$222,750 – US$371,250 pa

Hybrid

Medical Director, Oncology Clinical Development - Hematology

Serves as the physician within oncology clinical program teams, leading medical monitoring, safety oversight and clinical data interpretation for hematology studies. Partners with a Senior Scientist and cross-functional matrix teams on protocol development, regulatory interactions and investigator engagement, with hybrid working at least two days on-site.

GSK Baar Onyx US$222,750 – US$371,250 pa

Hybrid

Manager, Quality Clinical Risk Management

Independent clinical quality-risk leadership role translating risk signals into proactive mitigation, escalation and inspection readiness across trials and programs. Involves maintaining Clinical Quality Plans, driving risk monitoring reviews, advising on CAPA plans, and leading pre-submission quality portfolio reviews and mock inspections. Combines hands-on risk ownership with cross-functional influence and coaching of team members.

Johnson & Johnson Innovative Medicine High Wycombe

Hybrid

Senior Solutions Architect – Digital Experience & AI

Lead solution architecture for digital experience initiatives spanning web applications, APIs, content platforms and AI-enabled services, remaining hands-on through discovery, prototyping and architectural development. Bridge UX and engineering, translating user needs into accessible, sustainable architectures while providing technical direction and people management to the development team. Focus on LLMs, retrieval-augmented generation, agents and semantic search.

EMBL-EBI Saffron Walden

Hybrid Contract

Principal Clinical Database Programmer - eCOA

Designs, configures, tests and deploys electronic Clinical Outcome Assessment (eCOA) solutions for clinical trials, translating protocols and assessment schedules into questionnaires, branching logic, reminders and workflows. Works independently across multiple global studies, coordinating eCOA-to-EDC integration and supporting UAT, defect triage and post-production fixes. Also acts as a subject matter expert, trainer and technical contact for sponsors and cross-functional teams.

Parexel Sheffield

Remote Permanent

Bioinformatician – Structural Proteomics & Integrative Modelling

Develops FAIR infrastructure connecting proteomics evidence (XL-MS, CF-MS, AP-MS) with structural restraints, predicted structures and integrative models. Builds data models, APIs, conversion and validation tools with PRIDE and wwPDB, extending community standards for structural interactomics and linked deposition workflows.

EMBL-EBI Saffron Walden

Hybrid Contract